Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men - Test2 - elhamkhani - TriplyDB

Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men

Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men

http://www.wikidata.org/entity/Q24614084

about

New single nucleotide polymorphism G5508A in the SEPT12 gene may be associated with idiopathic male infertility in Iranian men.Single-nucleotide polymorphisms in the LRWD1 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome.

P2860

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P2860

Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men

http://www.wikidata.org/entity/Q24614084

description

2012 nî lūn-bûn

@nan

2012 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@ast

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@en

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@nl

type

label

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@ast

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@en

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@nl

prefLabel

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@ast

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@en

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@nl

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S10815-011-9679-5

P1433

Journal of Assisted Reproduction and Genetics

P1476

Single nucleotide polymorphism ...... meiotic arrest in Japanese men

@en

P2093

Akira Tsujimura

http://www.w3.org/2001/XMLSchema#string

Eitetsu Koh

http://www.w3.org/2001/XMLSchema#string

Kazuo Sengoku

http://www.w3.org/2001/XMLSchema#string

Michiharu Horikawa

http://www.w3.org/2001/XMLSchema#string

Mikio Namiki

http://www.w3.org/2001/XMLSchema#string

Toshinobu Miyamoto

http://www.w3.org/2001/XMLSchema#string

Yasuaki Saijo

http://www.w3.org/2001/XMLSchema#string

Yasushi Miyagawa

http://www.w3.org/2001/XMLSchema#string

P2860

Azoospermia in patients heterozygous for a mutation in SYCP3

SEPT12 interacts with SEPT6 and this interaction alters the filament structure of SEPT6 in Hela cells

Essential role of Fkbp6 in male fertility and homologous chromosome pairing in meiosis

MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice

The expression level of septin12 is critical for spermiogenesis

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene

Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10 mutations in oligozoospermic patients impair homodimerization

Mammalian MutS homologue 5 is required for chromosome pairing in meiosis

The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility

A histone H3 methyltransferase controls epigenetic events required for meiotic prophase

P2888

s10815-011-9679-5

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47-51

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scholarly article

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10.1007/S10815-011-9679-5

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P433

1

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29

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2012-01-01T00:00:00Z

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51829945

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P6179

1024696109

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P698

22116646

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P921

reproductive medicine

single-nucleotide polymorphism

obstetrics and gynaecology

P932

3252415

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